VWA8

von Willebrand factor A domain containing 8
OMIM: 617509, ClinGen, DECIPHER

2 panels

Panel Reviews Mode of inheritance Details
2 panels

Green VWA8 in Mendeliome


Version 1.4184

2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Green
  • Literature
Phenotypes
  • Retinitis pigmentosa 97, MIM#620422

Green VWA8 in Retinitis pigmentosa


Level 2: Ophthalmological disorders
Version 0.238

Component of the following Super Panels:

  • Retinal Disorders Superpanel
  • 2 reviews MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Literature
    • Expert Review Green
    • Expert Review Green
    • Literature
    Phenotypes
    • Retinitis pigmentosa 97, MIM#620422